Hs04385285_cn

• Gene Symbol: ZNF33B
• Assay Reference Genome Location: Chr.10:42631613 on build GRCh38
• Cytoband: 10q11.21

Target Gene Details

• Entrez Gene ID: 7582
• Gene Name: zinc finger protein 33B
• Gene Aliases: KOX2, KOX31, ZNF11B
• Location: Chr.10:42574169-42638837 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ZNF33B	NM_001305033.1			NP_001291962.1
	NM_001305035.1			NP_001291964.1
	NM_001305036.1			NP_001291965.1
	NM_001305037.1			NP_001291966.1
	NM_001305038.1			NP_001291967.1
	NM_001305039.1			NP_001291968.1
	NM_001305040.1			NP_001291969.1
	NM_006955.2			NP_008886.1
	NR_130948.1
	NR_130949.1
	NR_130950.1
	NR_130951.1
	AJ491697.1			CAD36956.1
	AK096683.1
	AK304306.1
	AK309564.1
	AK310073.1
	BC048313.2			AAH48313.1
	BC065181.1			AAH65181.1
	BC107726.1			AAI07727.1
	BG536481.1
	CD652356.1
	DA230792.1
	DA493121.1
	DA826003.1
	DA959465.1
	DB156590.1
	DR000119.1
	X68684.1			CAA48643.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
esv3623017	Chr.10:42584089 - 42655641 on Build GRCh38	Loss	ZNF33B
esv34929	Chr.10:42620746 - 42834322 on Build GRCh38	Loss	BMS1 LOC105378269 LOC283028 ZNF33B LINC01518
nsv1042764	Chr.10:42350935 - 43016264 on Build GRCh38	Gain	BMS1 ZNF37BP LOC441666 LOC105378269 MIR5100 CCNYL2 LINC01264 LOC101929445 LOC283028 ZNF33B LINC00839 LINC01518
nsv550672	Chr.10:42257742 - 42946281 on Build GRCh38	Gain	BMS1 ZNF37BP LOC441666 LOC105378269 CCNYL2 LOC101929445 LOC283028 ZNF33B LINC00839 LINC01518
esv2759746	Chr.10:42469683 - 43014743 on Build GRCh38	Loss	BMS1 ZNF37BP LOC105378269 MIR5100 CCNYL2 LINC01264 LOC101929445 LOC283028 ZNF33B LINC00839 LINC01518
esv3891795	Chr.10:42298677 - 42690427 on Build GRCh38	Gain	ZNF37BP LOC441666 CCNYL2 ZNF33B LINC00839 LINC01518
nsv469725	Chr.10:42469682 - 42682875 on Build GRCh38	Gain	ZNF37BP CCNYL2 ZNF33B LINC00839 LINC01518

More Information

Additional Information:

For this assay, SNP(s) [rs115395677] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

C2H2 zinc finger transcription factor

Gene Ontology Categories:

Process(es)

transcription, DNA-templated
regulation of transcription, DNA-templated

Function(s)

DNA binding
transcription factor activity, sequence-specific DNA binding
protein binding
metal ion binding